Preston-Hurlburt P, al-Ramadi B K, Rothbard J, Janeway C A
ImmuLogic Pharmaceutical Corporation, Palo Alto, California 94304.
Nature. 1992 Oct 1;359(6394):429-31. doi: 10.1038/359429a0.
T cells recognize foreign protein antigens in the form of peptide fragments bound tightly to the outer aspect of molecules encoded by the major histocompatibility complex (MHC). Most of the amino-acid differences that distinguish MHC allelic variants line the peptide-binding cleft, and different allelic forms of MHC molecules bind distinct peptides. It has been demonstrated that peptide-binding to MHC class I involves anchor residues in certain positions and that antigenic peptides associated with MHC class I exhibit allele-specific structural motifs. We have previously reported an analysis of MHC class II-associated peptide sequences. Here we extend this analysis and show that certain amino-acid residues occur at particular positions in the sequence of peptides binding to a given MHC class II molecule. These sequence motifs require the amino terminus to be shifted one or two positions to obtain alignment; such shifts occur naturally for a single peptide sequence without qualitatively altering CD4 T-cell recognition.
T细胞以紧密结合于主要组织相容性复合体(MHC)编码分子外侧的肽片段形式识别外来蛋白质抗原。区分MHC等位基因变体的大多数氨基酸差异位于肽结合裂隙处,并且MHC分子的不同等位基因形式结合不同的肽。已经证明,肽与MHC I类的结合涉及某些位置的锚定残基,并且与MHC I类相关的抗原肽表现出等位基因特异性结构基序。我们之前报道了对MHC II类相关肽序列的分析。在此,我们扩展了该分析,并表明某些氨基酸残基出现在与给定MHC II类分子结合的肽序列中的特定位置。这些序列基序要求氨基末端移位一或两个位置以获得比对;对于单个肽序列,这种移位自然发生,而不会定性改变CD4 T细胞识别。